Results 21 to 30 of about 9,561 (186)

Acquired hemophilia A (AHA): underreported, underdiagnosed, undertreated medical condition

The Egyptian Journal of Internal Medicine, 2022
Background Acquired hemophilia A (AHA) is a rare acquired bleeding disorder occurred due to the formation of inhibitory antibodies neutralizing endogenous factor VIII. Main body About half the cases are idiopathic.
Doaa M. El Demerdash, Alia Ayad, Noha Tawfik   +2 more
doaj   +1 more source

Postpartum-acquired hemophilia: A challenging disease to manage

Journal of Applied Hematology, 2017
Acquired hemophilia is a severe bleeding diathesis that affects both males and females. It is caused by suddenly appearing autoantibodies that interfere with the coagulation factor VIII activity.
Mohammed A Karish, Amr Hanbali, Hazzaa Al Zahrani, Rahaf Al Sahli   +3 more
doaj   +1 more source

Acquired factor VIII deficiency in prostate adenocarcinoma presenting as multiple hematomas and hemarthrosis

SAGE Open Medical Case Reports, 2020
Acquired hemophilia A or acquired factor VIII deficiency is a rare bleeding disorder due to the presence of autoantibodies to factor VIII. It has been associated with autoimmune conditions, certain medications, and malignancy. It has a high morbidity and
Akeem Lewis, Joe Joseph, Nirmal Pathak, Babak Baseri, Carol Luhrs   +4 more
doaj   +1 more source

Diagnosis and Treatment of Acquired Hemophilia A (AHA) with Bullous Pemphigoid

Jurnal Penyakit Dalam Indonesia, 2016
Acquired hemophilia A is a condition in which coagulation factor VIII become inactive due to autoantibody formation. This condition is related to pregnancy, malignancy, and autoimmune disease with skin disorder. In this case report, a 66 years woman with
Rasco Sandy Sihombing, Henry Ratno Diono Silalahi, Hamzah Shatri, Lugyanti Sukrisman, Ikhwan Rinaldi, Findy Prasetyawati, Endy Novianto, Em Yunir   +7 more
doaj   +1 more source

Acquired hemophilia A in the setting of dual anticoagulation therapy and lupus anticoagulant: a case report

Journal of Medical Case Reports, 2022
Background Acquired hemophilia A is a disorder caused by autoantibodies against coagulation factor VIII that may present with severe bleeding. We report a rare case of acquired hemophilia A presenting with coexisting lupus anticoagulant.
Victor Chen, Lauren C. Roby, Stephanie Wentzel, Mingjia Li, Nicholas Jones   +4 more
doaj   +1 more source

SUCCESSFUL LONG TERM ERADICATION OF FACTOR VIII INHIBITOR IN PATIENTS WITH ACQUIRED HAEMOPHILIA A IN SAUDI ARABIA

Mediterranean Journal of Hematology and Infectious Diseases, 2012
<p>Acquired haemophilia A is a serious and potentially fatal bleeding disorder. Diagnosis is difficult and maybe delayed due to its rarity. The high mortality rate and the complex nature of treatment necessitate patient management at a haemophilia ...
Galila F Zaher, Soheir S Adam
doaj   +3 more sources

[Acquired hemophilia]

Revista de la Facultad de Ciencias Medicas (Cordoba, Argentina), 2022
Acquired hemophilia is a hemostasis disorder that occurs due to the presence of inhibitory autoantibodies that are directed against coagulation factor VIII. Clinically, it is manifested by spontaneous bleeding mainly in the skin and soft tissues, and unlike hereditary hemophilia ,the presence of hemarthrosis is infrequent.
Martín, Milanesio, Aldo Hugo, Tabares, Gastón Andrés, Caeiro, Julieta, Olmedo, Ana Romina, Montivero   +4 more
openaire   +1 more source

Successful use of emicizumab in a patient with refractory acquired hemophilia A and acute coronary syndrome requiring percutaneous coronary intervention

Research and Practice in Thrombosis and Haemostasis, 2019
Essentials Acquired hemophilia A is a rare bleeding disorder often accompanied by other comorbidities. We describe emicizumab use in acquired hemophilia A complicated by acute coronary syndrome.
Kathryn E. Dane, John P. Lindsley, Michael B. Streiff, Alison R. Moliterno, Mian K. Khalid, Satish Shanbhag   +5 more
doaj   +1 more source

Acquired hemophilia in patient with Systemic lupus erythematosus: Clinical case report

Научно-практическая ревматология
Acquired hemophilia is a rare disease that develops because of the synthesis of antibodies to endogenous VIII blood clotting factor. The most common symptom of acquired hemophilia is spontaneous bleeding.
S. A. Alekseeva, N. I. Zozulya, T. M. Reshetnyak   +2 more
doaj   +1 more source

A Case of Acquired Hemophilia A in a Patient with Exposure to COVID-19

Case Reports in Hematology, 2022
Acquired Hemophilia A (AHA) is a very rare autoimmune condition involving immune-mediated depletion of Factor VIII, resulting in spontaneous hemorrhage.
Jorge D. Guerra, Jasmine Gowarty, Jordan Buess, James Mason, Kathleen Halka   +4 more
doaj   +1 more source